Cleared Traditional

K770654 - UN

K770654 is the FDA 510(k) clearance for UN by Bd Becton Dickinson Vacutainer Systems Preanalytic. It is a Class 2 Chemistry device (product code CDQ) cleared through the Traditional 510(k) pathway after a 79-day FDA review.

K770654 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Chemistry device
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Jun 1977
Decision
79d
Days
Class 2
Risk

K770654 is an FDA 510(k) clearance for the UN, UV DELTA TEST ASSAY. Classified as Urease And Glutamic Dehydrogenase, Urea Nitrogen (product code CDQ), Class II - Special Controls.

Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Washington, US). The FDA issued a Cleared decision on June 24, 1977 after a review of 79 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1770 - the FDA in vitro diagnostics and chemistry framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Bd Becton Dickinson Vacutainer Systems Preanalytic devices

Submission Details

510(k) Number K770654 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 06, 1977
Decision Date June 24, 1977
Days to Decision 79 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
9d faster than avg
Panel avg: 88d · This submission: 79d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code CDQ Urease And Glutamic Dehydrogenase, Urea Nitrogen
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1770
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - CDQ Urease And Glutamic Dehydrogenase, Urea Nitrogen

All 90
Devices cleared under the same product code (CDQ) and FDA review panel - the closest regulatory comparables to K770654.
BUN TEST UNI-UV BLOOD UREA NITROGEN TEST
K780943 · Sclavo, Inc. · Jul 1978
BUN REAGNET SET
K780069 · Medical Analysis Systems, Inc. · Feb 1978
FASTCHEM BUN
K771923 · Boehringer Mannheim Corp. · Nov 1977
BUN, ENZYMATIC
K770315 · Icn Pharmaceuticals, Inc. · Apr 1977
ENZYMATIC BUN (RATE) REAGENT KIT
K761261 · Beckman Instruments, Inc. · Dec 1976
ENZYMATIC BUN REAGENT KIT
K760414 · Beckman Instruments, Inc. · Nov 1976